{
    "disease_id": "DOID:0110215", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011473", 
            "name": "Leber congenital amaurosis caused by mutation in LCA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011473", 
            "name": "LCA5 Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011473", 
            "name": "LCA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011473", 
            "name": "Leber congenital amaurosis type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011473", 
            "name": "Leber congenital amaurosis 5; LCA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011473", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011473", 
            "name": "amaurosis congenita of Leber, type 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110215", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110215", 
            "name": "LCA5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110215", 
        "description": "A Leber congenital amaurosis that is characterized by severe visual dysfunction, nystagmus, the oculodigital sign, and a normal fundus with onset in infancy and has_material_basis_in mutation in the LCA5 gene on chromosome 6q14.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110215", 
        "name": "Leber congenital amaurosis 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110215#disease-associations", 
            "id": "0110215", 
            "database": "Alliance of Genome Resources"
        }
    ]
}